Prediction of protein assemblies, the next frontier: The CASP14-CAPRI experiment.
CAPRI
CASP
blind prediction
docking
oligomeric state
protein assemblies
protein complexes
protein docking
protein-protein interaction
template-based modeling
Journal
Proteins
ISSN: 1097-0134
Titre abrégé: Proteins
Pays: United States
ID NLM: 8700181
Informations de publication
Date de publication:
12 2021
12 2021
Historique:
revised:
24
07
2021
received:
20
05
2021
accepted:
05
08
2021
pubmed:
29
8
2021
medline:
26
2
2022
entrez:
28
8
2021
Statut:
ppublish
Résumé
We present the results for CAPRI Round 50, the fourth joint CASP-CAPRI protein assembly prediction challenge. The Round comprised a total of twelve targets, including six dimers, three trimers, and three higher-order oligomers. Four of these were easy targets, for which good structural templates were available either for the full assembly, or for the main interfaces (of the higher-order oligomers). Eight were difficult targets for which only distantly related templates were found for the individual subunits. Twenty-five CAPRI groups including eight automatic servers submitted ~1250 models per target. Twenty groups including six servers participated in the CAPRI scoring challenge submitted ~190 models per target. The accuracy of the predicted models was evaluated using the classical CAPRI criteria. The prediction performance was measured by a weighted scoring scheme that takes into account the number of models of acceptable quality or higher submitted by each group as part of their five top-ranking models. Compared to the previous CASP-CAPRI challenge, top performing groups submitted such models for a larger fraction (70-75%) of the targets in this Round, but fewer of these models were of high accuracy. Scorer groups achieved stronger performance with more groups submitting correct models for 70-80% of the targets or achieving high accuracy predictions. Servers performed less well in general, except for the MDOCKPP and LZERD servers, who performed on par with human groups. In addition to these results, major advances in methodology are discussed, providing an informative overview of where the prediction of protein assemblies currently stands.
Identifiants
pubmed: 34453465
doi: 10.1002/prot.26222
pmc: PMC8616814
mid: NIHMS1735921
doi:
Substances chimiques
Proteins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
1800-1823Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM136409
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : NIGMS NIH HHS
ID : R01 GM074255
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM109980
Pays : United States
Organisme : NIGMS NIH HHS
ID : R21 GM127952
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM118078
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM124952
Pays : United States
Organisme : Medical Research Council
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL142301
Pays : United States
Organisme : Cancer Research UK
ID : FC001003
Pays : United Kingdom
Organisme : NIGMS NIH HHS
ID : T32 GM132024
Pays : United States
Organisme : NIGMS NIH HHS
ID : RM1 GM135136
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM078221
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM123055
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM133840
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM093123
Pays : United States
Informations de copyright
© 2021 Wiley Periodicals LLC.
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